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FDA 510(k) Applications Submitted by DIANA L WOLANIUK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060964
04/07/2006
ARCHITECT BNP ASSAY, MODEL 8K28
FUJIREBIO DIAGNOSTICS, INC.
K052000
07/25/2005
ARCHITECT CA 19-9XR ASSAY
FUJIREBIO DIAGNOSTICS, INC.
K052889
10/13/2005
VITROS CA 19-9
FUJIREBIO DIAGNOSTICS, INC.
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